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Job Details

Contract CMP QA Auditor - Global Pharma - UK, North West - 3-6 Month Contract - Competitive Rest

Company: Meet
Location:
Reference: MD QA Aud NW
Closing Date: 13 Feb 17
Type: Contract
Salary (£): Competitive
Benefits:

Job Summary:

A global pharmaceutical company is looking for an experienced QA Auditor with experience pharmaceutical manufacturing within liquids, creams, ointments and solid-dose forms. This project is a 3-6 month contract and is a fantastic opportunity for a contractor to develop their career in this fast growing company. To find out more speak to Matt on 0203 019 6006 or email directly at matt@peoplewithchemistry.com to discuss in confidence.

Requirements:

A fantastic opportunity is available for an experienced QA Auditor with experience working within pharmaceutical manufacturing. Based at their UK site in the North West you will be responsible for planning and leading the audits at their CMO sites across the globe.

Suited to those that specialise in auditing or have 5 years experience performing internal and 3rd party audits within a QA role. The ideal candidate will need to be prepared to travel overseas for audits.

 

Get in touch with Matt Dixon at matt@peoplewithchemistry.com or call on 0203 019 6006 to find out more about this opportunity. This will be 100% confidential.

 

Company Background

My client is a medium sized pharmaceutical company that operate across Europe, USA and the rest of the world. The company has tripled in size over the last 9 years and are continuing to grow. This company manufactures pharmaceutical products across all dosage forms.

Role Responsibilities

Working as a QA Auditor your main responsibilities will be:

·         Develop and maintain an auditing profile for contract manufacturing organisations globally.

·         Organise the auditing schedule and complete the necessary follow up procedures including report writing.

·         Establish quality agreements between the client and the contract manufacturing organisations and ensure that the terms are met.

·         Devise rating metrics to analyse the performance of contract manufacturing organisations.

·         Perform audits of internal audits when applicable

·         Provide tech transfer support when necessary.

This role is ideal for a senior QA Officer that has experience working across a variety of manufacturing dosage forms including liquids, ointments and creams.

 

Get in touch with Matt Dixon at matt@peoplewithchemistry.com or call on 0203 019 6006 to find out more about this opportunity. This will be 100% confidential.

 

Skills Required

·         Bachelor's degree in science, engineering or related subject is essential.

·         Hands on GMP and GDP auditing experience in a leadership capacity.

·         Experience of working with a wide variety of dosage forms including liquids, ointments, creams and solid doses.

·         Will need to be able to work autonomously and provide leadership and mentoring for more junior colleagues.

·         Has the critical thinking and analytical capabilities to ensure the correct audit follow-up procedures take place.

·         Excellent verbal and written communication skills, ability to work well in teams or independently and the ability to prioritise work and manage multiple projects while maintaining quality and compliance.

 

Get in touch with Matt Dixon at matt@peoplewithchemistry.com or call on 0203 019 6006 to find out more about this opportunity. This will be 100% confidential.

 

Commutable Locations: UK, North West.

Rate: Competitive

 

Full job description and company details are available upon application, apply below. The position is being dealt with by Matt Dixon at Meet, call us on 0203 019 6006 or email directly at matt@peoplewithchemistry.com to discuss in confidence.

Meet are good people wo are great at recruitment. We’re proud to partner with the industry’s leading Pharmaceutical, Biotechnology, Medical Device, Marketing Communications and Contract Research Organisations (CROs) worldwide, helping them to find and secure the best global talent available. We pride ourselves on our open, friendly approach and are here to guide you through the recruitment process every step of the way.

Find out more about us at www.peoplewithchemistry.com https://uk.linkedin.com/in/matthew-dixon-34aab863

Key Words

Biopharmaceuticals, Biopharma, Bio-pharmaceuticals, Bio-pharma, QA, Quality Assurance, Quality Assurance Associate, Quality, GMP, GCP, GLP, GDP, GxP, liquids, ointmenst, creams, solid-dose, steriles, aseptic, CAPA, CAPAs, corrective action, preventative action, corrective and preventative action, drug development, clinical trials, manufacturing, phase one, phase two, phase three, phase four, UK, North West, North, CMO. 

Apply for this job: Contract CMP QA Auditor - Global Pharma - UK, North West - 3-6 Month Contract - Competitive Rest

Contact Information:

Address:  meet
Euston Tower Levels 32-34 286 Euston Road London
NW1 3DP
England
Tel:  +44 203 178 7488
Website:  Visit Our Web Site

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